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联合 Bentall 和改良 Ravitch 手术:病例报告和证据的系统评价。

Combined Bentall and Modified Ravitch Procedures: A Case Report and Systematic Review of the Evidence.

机构信息

Department of Cardiac Surgery, University Heart Center Dresden, 01307 Dresden, Germany.

Department of Pediatric Surgery, University Hospital Carl Gustav Carus, 01307 Dresden, Germany.

出版信息

Medicina (Kaunas). 2022 Nov 30;58(12):1774. doi: 10.3390/medicina58121774.

Abstract

: Marfan syndrome (MS) is a genetic disorder with autosomal dominant inheritance that affects the connective tissue and consequently many organ systems. The cardiovascular manifestations of MS are notorious and include aortic root dilatation or acute aortic dissection, which can cause morbidity and early mortality. However, surgical treatment of aortic pathology may be complicated by musculoskeletal deformity of the chest wall, as in pectus excavatum. In this regard, single-stage combined Bentall and Ravitch surgery is an extreme rarity that has also been scarcely reported in the literature. : We present the medical history and single-stage Bentall and modified Ravitch surgical treatment of an 18-year-old male MS patient with symptomatic and severe pectus excavatum (PEX) in conjunction with a pear-shaped aortic root aneurysm. To discuss our case in the context of a synopsis of similar published cases, we present a systematic review of combined Bentall surgical aortic aneurysm repair and Ravitch correction of PEX. : A total of four studies (one case series and three case reports) and a case from our institution describing a single-stage combined Bentall and Ravitch operation were included. Patients were 22 ± 5.9 years of age (median = 22.5 years) and predominantly male (60%). All cases reported a midline vertical skin incision over the sternum. The most common surgical approach was midsternotomy (80%). In all cases metal struts were used to reinforce the corrected chest wall. Postoperative mortality was zero. : Single-stage combined Bentall and Ravitch surgery is an underutilized surgical approach. Its use in MS patients with concomitant PEX and ascending aortic aneurysm that require surgical treatment warrants further investigation. Midsternotomy seems to be a viable access route that provides sufficient exposure in the single-stage surgical setting. Although operative time is long, the intraoperative and postoperative risks appear to be low and manageable.

摘要

马凡综合征(MS)是一种常染色体显性遗传的遗传疾病,影响结缔组织,进而影响许多器官系统。MS 的心血管表现是众所周知的,包括主动脉根部扩张或急性主动脉夹层,这可能导致发病率和早期死亡率。然而,由于胸壁骨骼畸形,如漏斗胸,主动脉病变的手术治疗可能会变得复杂。在这方面,一期联合 Bentall 和 Ravitch 手术极为罕见,在文献中也很少有报道。

我们报告了一名 18 岁男性 MS 患者的病史和一期 Bentall 和改良 Ravitch 手术治疗,该患者患有症状性和严重的漏斗胸(PEX),同时伴有梨形主动脉根部动脉瘤。为了在类似已发表病例的综述背景下讨论我们的病例,我们对联合 Bentall 手术治疗主动脉瘤修复和 Ravitch 矫正 PEX 进行了系统回顾。

共有四项研究(一项病例系列和三项病例报告)和我们机构的一项研究描述了一期联合 Bentall 和 Ravitch 手术,包括在内。患者年龄为 22 ± 5.9 岁(中位数 = 22.5 岁),主要为男性(60%)。所有病例均报告在胸骨正中线上有一条垂直的皮肤切口。最常见的手术入路是正中劈开胸骨(80%)。所有病例均使用金属支柱来加强矫正后的胸壁。术后死亡率为零。

一期联合 Bentall 和 Ravitch 手术是一种未充分利用的手术方法。在需要手术治疗的同时患有 PEX 和升主动脉瘤的 MS 患者中,其应用值得进一步研究。正中劈开胸骨似乎是一种可行的入路,可以在一期手术中提供足够的暴露。虽然手术时间较长,但术中及术后风险似乎较低且可控。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d219/9788579/2b88ca8edaf8/medicina-58-01774-g001.jpg

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